Capillary electrophoresis as a nanoreactor of separation capability: On‐capillary reaction catalyzed by transition metal ions
| Autor: | Tomoe Yamashiro, Tetsuo Okada |
|---|---|
| Rok vydání: | 2003 |
| Předmět: |
Tiron
Metal ions in aqueous solution Clinical Biochemistry Inorganic chemistry Electrophoresis Capillary Equipment Design Biochemistry Catalysis Analytical Chemistry Metal chemistry.chemical_compound Capillary length Capillary electrophoresis chemistry Catalytic oxidation Metals visual_art visual_art.visual_art_medium Nanotechnology Microreactor |
| Zdroj: | ELECTROPHORESIS. 24:2168-2173 |
| ISSN: | 1522-2683 0173-0835 |
| DOI: | 10.1002/elps.200305406 |
| Popis: | The catalytic oxidation of 1,2-dihydroxy-benzene-3,6-disulfonate (tiron) by metal ions has been studied for detection of the metal ions in capillary electrophoresis (CE). Although Co 2 + shows the strongest catalytic capability, some other metal ions also catalyze this reaction. If metal ions encounter a H 2 O 2 zone after electrophoretic separation in the running buffer containing tiron, tiron is catalytically oxidized while the metal ion passes through the H 2 O 2 zone. Anionic tiron radicals produced by the reaction are finally measured by the detector; in this scheme, the capillary acts as a nano- or microreactor as well as a microseparator. The effective capillary length can be controlled by changing the interval between metal ion and H 2 O 2 injections. This scheme has been successfully applied to the detection of Co 2 + , Cu 2 + , Mn 2 + , and VO 2 + . The detectability is discussed from several viewpoints, such as the intrinsic catalyst ability of metal ions, the kinetics of the catalytic reaction, and reaction times determined by the mobility of the zone of the metal ion. Some strange behaviors, which cannot be predicted by batch experiments, are also reported. |
| Databáze: | OpenAIRE |
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